Onapristone and Anastrozole for the Treatment of Refractory Hormone Receptor Positive Endometrial Cancer

Refractory Endometrial Carcinoma Clinical Trial

Official title:

A Phase II Clinical Trial Evaluating the Combination of Onapristone With Anastrozole for Women With Refractory Hormone Receptor Positive Endometrial Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04719273
• Other study ID #: 20P.829
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: January 28, 2021
• Est. completion date: December 31, 2024

Study information

• Verified date: March 2024
• Source: Thomas Jefferson University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase II trial studies the effect of onapristone and anastrozole in treating patients with hormone receptor positive endometrial cancer that has not responded to previous treatment (refractory). Progesterone and estrogen are hormones that can cause the growth of endometrial cancer cells. Onapristone blocks the use of progesterone by the tumor cells. Anastrozole is a drug that blocks the production of estrogen in the body. Giving onapristone with anastrozole may work better than anastrozole alone in treating patients with hormone receptor positive endometrial cancer.

Description:

PRIMARY OBJECTIVE:

I. To evaluate the activity and safety of a pure progesterone receptor (PR) antagonist, extended-release onapristone (onapristone), with anastrozole to treat women with recurrent metastatic estrogen receptor positive (ER+)/progesterone receptor positive (PR+) endometrial carcinoma.

SECONDARY OBJECTIVES:

I. To estimate the disease control rate (DCR). II. To describe duration of response (DOR). III. To evaluate the safety and tolerability. IV. To evaluate quality of life using the Edmonton Symptom Assessment questionnaire.

EXPLORATORY OBJECTIVES:

I. To characterize the ER and PR expression by immunohistochemistry (IHC) pre- and post-treatment.

OUTLINE:

Patients receive onapristone orally (PO) twice daily (BID) and anastrozole PO once daily (QD) on days 1-28. Treatment repeats every 28 days for up to 24 cycles (24 months) in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 3 months for up to 1 year after last treatment administration.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 14
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age greater than or equal to 18 years old

• Histologically confirmed diagnosis of endometrial cancer with ER and/or PR expression >= 1% by IHC on archival tissue taken within the prior 3 years or new biopsy if no archival tissue is available. IHC results do not have to be from Thomas Jefferson University

• Patients who have failed one prior treatment with a platinum/taxane chemotherapy regimen for management of disease

• Patients cannot have treatment with more than 2 prior lines of therapy (one line must be platinum/taxane regimen)

• Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version (v.)1.1. Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension. Each lesion must be >= 10 mm when measured by computed tomography (CT) or magnetic resonance imaging (MRI). Lymph nodes must be >= 15 mm in short axis when measured by CT or MRI

• Patients with the following histologic epithelial cell types are eligible:

• Endometrioid adenocarcinoma

• Serous adenocarcinoma

• Undifferentiated carcinoma

• Clear cell adenocarcinoma

• Mixed epithelial carcinoma

• Adenocarcinoma not otherwise specified (NOS)

• Please note: patients with carcinosarcoma are ineligible for this trial

• Patients must have had one prior treatment with a platinum/taxane chemotherapy regimen for management of disease

• Eastern Cooperative Oncology Group (ECOG) performance status 0-1

• Must have a life expectancy of at least 12 weeks as judged by the treating physician

• Females are only eligible for this study if they are postmenopausal. This is defined as meeting one of the following criteria:

• S/p total abdominal hysterectomy and bilateral salpingo-oopherectomy

• Patients who are in menopause is defined clinically as 12 consecutive months of amenorrhea in a woman over 55 in the absence of other biological or physiological causes OR women under the age of 55 must have a documented serum follicle stimulating hormone (FSH) level less than 40 mIU/mL.

• Body weight > 30 kg

• Absolute neutrophil count 1500/ul or more

• Platelets 100,000/ul or more

• Hemoglobin 9 g/dl or more

• Bilirubin less than or equal to 1.5 x the upper limit of normal (except subjects with Gilbert syndrome, who can have total bilirubin < 3 mg/dl)

• Endocrine and targeted therapy protocols usually enroll patients with aspartate aminotransferase (AST)/alanine aminotransferase (ALT) < 2.5 x upper limit of normal (ULN) in patients without underlying liver metastasis and < 5.0 x ULN in patients with underlying liver metastasis

• Glomerular filtration rate (GFR) greater than or equal to 40 ml/min using the Cockcroft-Gault formula or measured creatinine clearance using 24 hours urine collection

• International normalized ratio (INR) OR prothrombin time (PT) and activated partial thromboplastin time (aPTT) =< 1.5 x ULN unless participant is receiving anticoagulant therapy as long as PT or aPTT is within therapeutic range of intended use of anticoagulants

• All subjects must be able to comprehend and sign a written informed consent document

• Resolution of all acute toxic effects of prior therapy to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) (version 5.0) grade =< 1, with the exception of unresolved grade 2 neuropathy and grade 2 alopecia, which are allowed

• Patient has recovered from any prior radiotherapy

• Patients must be able to swallow tablets whole, without crushing

• Be able to read and speak English

Exclusion Criteria:

• Concurrent or recent chemotherapy, radiotherapy, immunotherapy, or general anesthesia/major surgery within 3 weeks

• History of prior hormonal therapy (i.e., megestrol acetate, tamoxifen or aromatase inhibitors) for treatment cancer within the past 2 months. Other concurrent hormonal therapy will not be allowed on this trial

• Patient has a concurrent malignancy or history of invasive malignancy within 3 years of enrollment, with the exception of basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the cervix that has completed curative therapy

• If participant received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting study treatment

• Has received prior systemic anti-cancer therapy including investigational agents within 3 weeks prior to randomization

• Known brain metastasis which have not been treated or showed stability for >= 6 months

• Proteinuria > 1+ on urinalysis or > 1 gm/24 hours (hr)

• Known history of New York Heart Association stage 3 or 4 cardiac disease

• A pleural or pericardial effusion of greater than or equal to grade 3 severity

• Women who are pregnant or nursing

• Has an active infection requiring systemic therapy

• Use of any prescription medication during the prior 28 days of first onapristone dosing that the investigator judges is likely to interfere with onapristone activity; specifically strong inhibitors or inducers, or sensitive substrates of cytochrome P450 CYP3A4

• Patients may not be on a concurrent clinical trial, unless approved by investigator

Related Conditions & MeSH terms

• Adenocarcinoma
• Carcinoma
• Carcinoma, Endometrioid
• Endometrial Neoplasms
• Refractory Endometrial Adenocarcinoma
• Refractory Endometrial Carcinoma
• Refractory Endometrial Clear Cell Adenocarcinoma
• Refractory Endometrial Endometrioid Adenocarcinoma
• Refractory Endometrial Mixed Cell Adenocarcinoma
• Refractory Endometrial Serous Adenocarcinoma
• Refractory Endometrial Undifferentiated Carcinoma

Intervention

Drug:
• Extended-release Onapristone
Given PO
• Anastrozole
Given PO

Other:
• Quality-of-Life Assessment
Ancillary studies
• Questionnaire Administration
Ancillary studies

Diagnostic Test:
• Estrogen Receptor Positive (Positive Estrogen Receptor; ESR Positive; ESR1 Positive; ER Positive; Estrogen Receptor Alpha Positive)
Immunohistochemistry (IHC):Integral : Tissue
• Progesterone Receptor Positive ( PGR Positive; PR Positive)
Immunohistochemistry (IHC)

Locations

Country	Name	City	State
United States	Jefferson Abington Hospital	Abington	Pennsylvania
United States	Thomas Jefferson University	Philadelphia	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
Thomas Jefferson University	Context Therapeutics Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Estrogen receptor and progesterone receptor expression	Assessed by immunohistochemistry and represented as a percentage prior to trial initiation and at progression.	Up to 1 year post-treatment
Primary	Objective response rate (ORR)	Defined by the percentage of patients with tumor response (complete response [CR] or partial response [PR]) as defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.	Up to 1 year post-treatment
Primary	Progression-Free Survival (PFS)	4 month PFS is defined as a binary endpoint, from first dose of onapristone and anastrozole to 4 months of therapy as "confirmed progression-free" or "not progression-free" (including cancer progression or censored subjects). Will use the date of first documented disease progression or recurrence, as assessed by using RECIST 1.1 criteria, or death due to any cause, whichever occurs first.	At 4 months
Secondary	Disease Control Rate	Defined as best overall response of CR, PR, or stable disease lasting for >= 24 weeks, per RECIST 1.1.	Up to 1 year post-treatment
Secondary	Time to Response		From randomization to first documented response (CR or PR) in months, assessed up to 1 year post-treatment
Secondary	Duration of Response		From the first date of documented response to progression or death due to endometrial cancer, assessed up to 1 year post-treatment
Secondary	Type, frequency and severity of adverse events and laboratory abnormalities	Adverse events will be graded for severity according to the Common Terminology Criteria for Adverse Events version 5.0.	Up to 30 days post-treatment
Secondary	Quality of Life and pain score	Quality of life and pain scores are defined by the Edmonton Symptom Assessment System using nine subjective patient measures of well-being including pain, tiredness, nausea, depression, anxiety, drowsiness, appetite, well-being, shortness of breath.	Up to 1 year post-treatment